Allele Registry

Canonical Allele Identifier: PA2825113444

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV003586768

ClinVar Variation:

2708702

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Glu1772Asp	CA389035854 NM_000257.4:c.5316G>T CA389035856 NM_000257.4:c.5316G>C